在Cr-MIL-101中探测N-捐赠分子与开放金属位点的相互作用:固态NMR光谱和密度功能理论研究
Thomas Wittmann1, Arobendo Mondal2, Carsten B L Tschense1
1Inorganic Chemistry III, University of Bayreuth , Universitätsstraße 30, 95447 Bayreuth, Germany.
Journal of the American Chemical Society
|January 10, 2018
概括
研究人员使用先进的NMR光谱和DFT计算来了解不同分子如何与Cr-MIL-101金属有机框架 (MOF) 的开放金属位点结合. 这揭示了对MOF设计至关重要的具体约束性偏好.
科学领域:
- 材料科学
- 固态化学
- 光谱学
背景情况:
- 控制金属有机框架 (MOF) 的特性依赖于了解主机-客户互动.
- 由于与易斯基本客体的强相互作用,MOF中的开放金属位点表现出选择性吸附.
研究的目的:
- 阐明水,阿米诺皮里丁和二甲与Cr-MIL-101中的开放金属位点之间的相互作用.
- 为这些客人建立一个有约束力的优先顺序.
主要方法:
- 采用C MAS NMR光谱法,用于高分辨率的光谱.
- 使用密度函数理论 (DFT) 计算来验证实验结果.
- 应用自旋格子放松和REDOR光谱编辑用于光谱赋值.
主要成果:
- 在开放的金属位点提供了每个客分子的独特特征.
- 竞争实验确定了结合偏好:水<二氨基胺><3氨基胺.
- 对Cr-MIL-101衍生物的实验数据进行验证的DFT计算的NMR转移.
结论:
- 结合NMR光谱和DFT计算有效地分配和确定开放金属场所的客体排列.
- NMR数据提供了客户和框架动态的洞察力,补充了结构信息.
- 该策略适用于研究MOF中的吸附剂混合物,有助于结构-性质关系的发展.
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